A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694536



Internal ID15431188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:71112759..71168036hg38UCSC Ensembl
Innerchr1:71578442..71633719hg19UCSC Ensembl
Innerchr1:71351030..71406307hg18UCSC Ensembl
Innerchr1:71290463..71345740hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3855278
hg1955278
hg1855278
hg1755278
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521769
Supporting Variants
Samples
Known GenesZRANB2-AS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694536
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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